PL2134685T3 - Pochodne indolu niepodstawione w pozycji 7 jako inhibitory Mcl-1 - Google Patents
Pochodne indolu niepodstawione w pozycji 7 jako inhibitory Mcl-1Info
- Publication number
- PL2134685T3 PL2134685T3 PL08745934T PL08745934T PL2134685T3 PL 2134685 T3 PL2134685 T3 PL 2134685T3 PL 08745934 T PL08745934 T PL 08745934T PL 08745934 T PL08745934 T PL 08745934T PL 2134685 T3 PL2134685 T3 PL 2134685T3
- Authority
- PL
- Poland
- Prior art keywords
- nonsubstituted
- mcl
- inhibitors
- indole derivatives
- indole
- Prior art date
Links
- 101001056180 Homo sapiens Induced myeloid leukemia cell differentiation protein Mcl-1 Proteins 0.000 title 1
- 102100026539 Induced myeloid leukemia cell differentiation protein Mcl-1 Human genes 0.000 title 1
- 229940054051 antipsychotic indole derivative Drugs 0.000 title 1
- 150000002475 indoles Chemical class 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
- C07D209/42—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/04—Immunostimulants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/06—Antianaemics
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
Landscapes
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Hematology (AREA)
- Immunology (AREA)
- Diabetes (AREA)
- Oncology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Indole Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US91204907P | 2007-04-16 | 2007-04-16 | |
| US94968307P | 2007-07-13 | 2007-07-13 | |
| PCT/US2008/060427 WO2008130970A1 (fr) | 2007-04-16 | 2008-04-16 | Inhibiteurs mcl-1 indole 7-non-substitués |
| EP08745934.3A EP2134685B1 (fr) | 2007-04-16 | 2008-04-16 | Derivés d'indole non-substitués en position 7 en tant qu'inhibiteurs de mcl-1 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL2134685T3 true PL2134685T3 (pl) | 2016-02-29 |
Family
ID=39683700
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL08745934T PL2134685T3 (pl) | 2007-04-16 | 2008-04-16 | Pochodne indolu niepodstawione w pozycji 7 jako inhibitory Mcl-1 |
Country Status (11)
| Country | Link |
|---|---|
| US (2) | US7981888B2 (fr) |
| EP (1) | EP2134685B1 (fr) |
| JP (2) | JP5496876B2 (fr) |
| CN (1) | CN101711235A (fr) |
| CA (2) | CA2682354C (fr) |
| DK (1) | DK2134685T3 (fr) |
| ES (1) | ES2550753T3 (fr) |
| MX (1) | MX2009011210A (fr) |
| PL (1) | PL2134685T3 (fr) |
| PT (1) | PT2134685E (fr) |
| WO (1) | WO2008130970A1 (fr) |
Families Citing this family (48)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2682356C (fr) | 2007-04-16 | 2016-06-14 | Abbott Laboratories | Inhibiteurs mcl-1 indole 7-substitues |
| CN102307862A (zh) * | 2008-12-08 | 2012-01-04 | 贝林格尔.英格海姆国际有限公司 | 用于治疗癌症的化合物 |
| NZ593537A (en) * | 2008-12-19 | 2013-07-26 | Genentech Inc | Isoquinoline derivatives and methods of use |
| ES2462715T3 (es) | 2008-12-19 | 2014-05-26 | Genentech, Inc. | Compuestos y métodos de uso |
| EP3138838A1 (fr) | 2010-01-29 | 2017-03-08 | Dana-Farber Cancer Institute, Inc. | Petites molécules pour la modulation de mcl-1 et procédés de modulation de la mort cellulaire, la division cellulaire, la différenciation cellulaire et procédés de traitement de troubles |
| EP2487159A1 (fr) | 2011-02-11 | 2012-08-15 | MSD Oss B.V. | Inhibiteurs du RORgammaT |
| EP2567698B1 (fr) | 2011-09-07 | 2014-02-12 | Rheinische Friedrich-Wilhelms-Universität Bonn | Agonistes de GPR 17 et analyse de criblage |
| US8940737B2 (en) | 2011-10-14 | 2015-01-27 | Abbvie Inc. | Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases |
| CA2868081C (fr) | 2012-03-20 | 2021-01-05 | Loren D. Walensky | Inhibition de mcl-1 et/ou de bfl-1/a1 |
| WO2014026330A1 (fr) * | 2012-08-15 | 2014-02-20 | Merck Sharp & Dohme Corp. | Composés 3-aminocycloalkyles en tant qu'inhibiteurs de rorgammat et leurs utilisations |
| WO2014026329A1 (fr) | 2012-08-15 | 2014-02-20 | Merck Sharp & Dohme Corp. | Composés d'indazole et d'indole n-alkylés en tant qu'inhibiteurs de rorgammat et leurs utilisations |
| WO2014026327A1 (fr) | 2012-08-15 | 2014-02-20 | Merck Sharp & Dohme Corp. | Composés d'acide benzoïque à substitution 4-hétéroaryle en tant qu'inhibiteurs de rorgammat et leurs utilisations |
| US10093640B2 (en) | 2012-09-21 | 2018-10-09 | Vanderbilt University | Substituted benzofuran, benzothiophene and indole MCL-1 inhibitors |
| CA2922341C (fr) | 2013-08-28 | 2022-06-07 | Vanderbilt University | Inhibiteurs de mcl-1 de type indole substitue |
| US10533010B2 (en) | 2014-03-27 | 2020-01-14 | Vanderbilt University | Substituted indole Mcl-1 inhibitors |
| US9949965B2 (en) | 2014-10-17 | 2018-04-24 | Vanderbilt University | Tricyclic indole Mcl-1 inhibitors and uses thereof |
| US20180291373A1 (en) | 2014-10-29 | 2018-10-11 | The Walter And Eliza Hall Institute Of Medical Research | Use of therapeutic agents |
| JP2018510135A (ja) | 2015-02-11 | 2018-04-12 | メルク・シャープ・アンド・ドーム・コーポレーションMerck Sharp & Dohme Corp. | RORγT阻害剤としての置換ピラゾール化合物及びその使用 |
| WO2016200726A1 (fr) | 2015-06-08 | 2016-12-15 | Texas Tech University System | Inhibiteurs de mcl-1 utilisés en tant que médicaments pour surmonter une résistance aux inhibiteurs de braf et inhibiteurs de mek |
| CA3002850A1 (fr) | 2015-10-27 | 2017-05-04 | Merck Sharp & Dohme Corp. | Composes indazole substitues utilises en tant qu'inhibiteurs de rorgammat et utilisations associees |
| WO2017075178A1 (fr) | 2015-10-27 | 2017-05-04 | Merck Sharp & Dohme Corp. | Composés pyrazoles bicycliques substitués en tant qu'inhibiteurs de rorgammat et leurs utilisations |
| CA3002853A1 (fr) | 2015-10-27 | 2017-05-04 | Merck Sharp & Dohme Corp. | Acides benzoiques a substitution heteroaryle en tant qu'inhibiteurs de rorgammat et leurs utilisations |
| EP3371173A4 (fr) * | 2015-11-02 | 2019-06-19 | Carmel-Haifa University Economic Corporation Ltd. | Composés mimétiques de protéine liée à l'apoptose dans la voie de signalisation de tgf-beta (arts), compositions, méthodes et utilisations correspondants dans l'induction de la différentiation et/ou de l'apoptose de cellules précancéreuses et malignes, rétablissant ainsi leur phénotype de type normal |
| KR102396177B1 (ko) * | 2016-03-04 | 2022-05-09 | 반더빌트유니버시티 | 치환된 인돌 mcl-1 억제제 |
| PE20181803A1 (es) | 2016-04-22 | 2018-11-19 | Astrazeneca Ab | Inhibidores de mcl-1 macrociclicos para tratar el cancer |
| EP3458459B1 (fr) | 2016-05-19 | 2022-04-27 | Bayer Aktiengesellschaft | Derivés d'indole macrocycliques |
| WO2017198341A1 (fr) | 2016-05-19 | 2017-11-23 | Bayer Aktiengesellschaft | Dérivés d'indole macrocycliques |
| JP6910027B2 (ja) * | 2017-03-29 | 2021-07-28 | 株式会社コーセー | チロシナーゼ活性阻害剤、メラニン産生抑制剤及び美白剤 |
| TW201841888A (zh) * | 2017-04-30 | 2018-12-01 | 財團法人生物技術開發中心 | 一種抗癌幹性之藥物 |
| US11447504B2 (en) | 2017-11-17 | 2022-09-20 | Bayer Aktiengesellschaft | Macrocyclic chlorine substituted indole derivatives |
| CN111757884B (zh) | 2017-11-17 | 2023-12-19 | 拜耳股份公司 | 取代的大环吲哚衍生物 |
| US20210253598A1 (en) | 2017-11-17 | 2021-08-19 | Bayer Aktiengesellschaft | Aryl annulated macrocyclic indole derivatives |
| US11478451B1 (en) | 2017-11-17 | 2022-10-25 | Bayer Aktiengesellschaft | Macrocyclic chlorine substituted indole derivatives |
| WO2019096911A1 (fr) | 2017-11-17 | 2019-05-23 | The Broad Institute, Inc. | Dérivés d'indole macrocycliques |
| EP3710449B1 (fr) | 2017-11-17 | 2022-07-06 | The Broad Institute, Inc. | Dérivés d'indole macrocycliques substitués par du fluor utilisés en tant qu'inhibiteurs de mcl-1, destinés à être utilisés dans le traitement du cancer |
| BR112021004805A2 (pt) * | 2018-09-30 | 2021-06-01 | Jiangsu Hengrui Medicine Co., Ltd. | derivado macrocíclico de indol, método de preparação do mesmo e aplicação do mesmo na medicina |
| WO2020103864A1 (fr) * | 2018-11-22 | 2020-05-28 | Ascentage Pharma (Suzhou) Co., Ltd. | Indoles macrocycliques servant d'inhibiteurs de mcl-1 |
| WO2020236556A1 (fr) | 2019-05-17 | 2020-11-26 | The Broad Institute, Inc. | Procédés de préparation d'indoles macrocycliques |
| WO2021092061A1 (fr) * | 2019-11-08 | 2021-05-14 | Unity Biotechnology, Inc. | Polythérapie pour le traitement de maladies associées à la sénescence |
| WO2021092053A1 (fr) * | 2019-11-08 | 2021-05-14 | Unity Biotechnology, Inc. | Composés macrocycliques inhibiteurs de mcl-1 destinés à être utilisées dans la gestion clinique d'états pathologiques provoqués ou induits par des cellules sénescentes ainsi que dans le traitement du cancer |
| WO2021099579A1 (fr) | 2019-11-21 | 2021-05-27 | Janssen Pharmaceutica Nv | Dérivés indoles macrocycliques utilisés comme inhibiteurs de la mcl-1 |
| JP2023502692A (ja) | 2019-11-21 | 2023-01-25 | ヤンセン ファーマシューティカ エヌ.ベー. | Mcl-1阻害剤としての大環状スルホニル誘導体 |
| JPWO2021107125A1 (fr) | 2019-11-29 | 2021-06-03 | ||
| CN115335384B (zh) * | 2020-03-30 | 2024-10-22 | 江苏恒瑞医药股份有限公司 | 一种吲哚类大环衍生物的结晶形式及其制备方法 |
| MX2022015005A (es) | 2020-05-29 | 2023-01-04 | Janssen Pharmaceutica Nv | Derivados de 7-pirazol-5-il-indol macrociclicos como inhibidores de mcl-1. |
| EP4168412A1 (fr) | 2020-06-19 | 2023-04-26 | JANSSEN Pharmaceutica NV | Dérivés de 7-(pyrazol-5-yl)-indole à liaison n en tant qu'inhibiteurs de mcl-1 |
| JP2024520801A (ja) | 2021-06-11 | 2024-05-24 | ギリアード サイエンシーズ, インコーポレイテッド | Mcl-1阻害剤と抗がん剤との組み合わせ |
| TWI861509B (zh) | 2021-06-11 | 2024-11-11 | 美商基利科學股份有限公司 | Mcl-1抑制劑與抗體藥物接合物之組合 |
Family Cites Families (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3632805A (en) | 1967-12-08 | 1972-01-04 | Sumitomo Chemical Co | Process for producing 1-aminoalkyl-benzodiazepine derivatives |
| FR2187318B1 (fr) | 1972-06-08 | 1975-06-20 | Delalande Sa | |
| US4994477A (en) * | 1988-03-24 | 1991-02-19 | Abbott Laboratories | Heterocyclic renin inhibitors |
| KR100482268B1 (ko) * | 1996-08-01 | 2005-04-14 | 메르클레 게엠베하 | 세포질 포스포리파제 a2의 저해제로서의 아실피롤디카르복실산 |
| GB9716657D0 (en) * | 1997-08-07 | 1997-10-15 | Zeneca Ltd | Chemical compounds |
| DE69929720T2 (de) | 1998-11-27 | 2006-09-21 | Mitsubishi Chemical Corp. | Verfahren zur Herstellung von Maleinsäureanhydrid |
| GB9902452D0 (en) * | 1999-02-05 | 1999-03-24 | Zeneca Ltd | Chemical compounds |
| GB9902455D0 (en) * | 1999-02-05 | 1999-03-24 | Zeneca Ltd | Chemical compounds |
| GB0000626D0 (en) * | 2000-01-13 | 2000-03-01 | Zeneca Ltd | Chemical compounds |
| US6787651B2 (en) * | 2000-10-10 | 2004-09-07 | Smithkline Beecham Corporation | Substituted indoles, pharmaceutical compounds containing such indoles and their use as PPAR-γ binding agents |
| DE10153346A1 (de) * | 2001-10-29 | 2004-04-22 | Grünenthal GmbH | Substituierte Indole |
| JP2005516908A (ja) * | 2001-11-30 | 2005-06-09 | ザ バーナム インスティチュート | 癌細胞におけるアポトーシスの誘導 |
| EP1513522A2 (fr) * | 2002-01-18 | 2005-03-16 | Sri International | Procedes pour traiter des pathologies associees a un recepteur d'edg |
| AU2003239150A1 (en) * | 2002-04-23 | 2003-11-10 | Aventis Pharmaceuticals Inc. | 3-substituted amino-1h-indole-2-carboxylic acid and 3-substituted amino-benzo |
| JP4695588B2 (ja) | 2003-02-26 | 2011-06-08 | スージェン, インク. | プロテインキナーゼ阻害剤としてのアミノヘテロアリール化合物 |
| WO2004092346A2 (fr) * | 2003-04-15 | 2004-10-28 | The Regents Of The University Of California | Inhibition par petites molecules d'une interaction de domaine pdz |
| SE0302035D0 (sv) * | 2003-07-09 | 2003-07-09 | Biolipox Ab | New compound |
| US7268159B2 (en) * | 2003-09-25 | 2007-09-11 | Wyeth | Substituted indoles |
| ITMI20040874A1 (it) * | 2004-04-30 | 2004-07-30 | Ist Naz Stud Cura Dei Tumori | Derivati indolici ed azaindolici con azione antitumorale |
| KR20070029809A (ko) * | 2004-06-18 | 2007-03-14 | 바이올리폭스 에이비 | 염증치료에 유용한 인돌 |
| DE602005014233D1 (de) * | 2004-06-18 | 2009-06-10 | Biolipox Ab | Zur behandlung von entzündungen geeignete indole |
| BRPI0512252A (pt) * | 2004-06-18 | 2008-02-19 | Biolipox Ab | composto ou um sal farmaceuticamente aceitável do mesmo, formulação farmacêutica, uso de um composto, método de tratamento de uma doença, produto combinado, e, processo para a preparação de um composto |
| WO2006041961A1 (fr) * | 2004-10-05 | 2006-04-20 | GOVERNMENT OF THE UNITED STATES OF AMERICA, as represented by THE SECRETARY, DEPARTMENT OF HEALTHAND HUMAN SERVICES | Inhibiteurs de la polymerisation de la tubuline de type arylthioindole, et procedes pour traiter ou prevenir un cancer au moyen de ces inhibiteurs |
| FR2878849B1 (fr) * | 2004-12-06 | 2008-09-12 | Aventis Pharma Sa | Indoles substitues, compositions les contenant, procede de fabrication et utilisation |
| JP2008527030A (ja) * | 2005-01-19 | 2008-07-24 | バイオリポックス エービー | 炎症の治療に有用なインドール類 |
| CA2593155A1 (fr) * | 2005-01-19 | 2006-07-27 | Biolipox Ab | Indoles utiles dans le traitement de l'inflammation |
| US7750004B2 (en) * | 2005-07-07 | 2010-07-06 | Abbott Laboratories | Apoptosis promoters |
| CL2007002516A1 (es) * | 2006-08-31 | 2008-05-16 | Smithkline Beecham Corp | Compuestos derivados de indol indano; composicion farmaceutica; y su uso para tratar hiperglicemia, diabetes tipo 2, tolerancia deteriorada a la glucosa, resistencia a la insulina, sindrome x, dislipidemia. |
| CA2682356C (fr) | 2007-04-16 | 2016-06-14 | Abbott Laboratories | Inhibiteurs mcl-1 indole 7-substitues |
| NZ593537A (en) | 2008-12-19 | 2013-07-26 | Genentech Inc | Isoquinoline derivatives and methods of use |
| ES2462715T3 (es) | 2008-12-19 | 2014-05-26 | Genentech, Inc. | Compuestos y métodos de uso |
-
2008
- 2008-04-16 CA CA2682354A patent/CA2682354C/fr active Active
- 2008-04-16 CN CN200880020451A patent/CN101711235A/zh active Pending
- 2008-04-16 JP JP2010504205A patent/JP5496876B2/ja not_active Expired - Fee Related
- 2008-04-16 WO PCT/US2008/060427 patent/WO2008130970A1/fr not_active Ceased
- 2008-04-16 US US12/104,319 patent/US7981888B2/en active Active
- 2008-04-16 ES ES08745934.3T patent/ES2550753T3/es active Active
- 2008-04-16 DK DK08745934.3T patent/DK2134685T3/en active
- 2008-04-16 PL PL08745934T patent/PL2134685T3/pl unknown
- 2008-04-16 EP EP08745934.3A patent/EP2134685B1/fr active Active
- 2008-04-16 MX MX2009011210A patent/MX2009011210A/es active IP Right Grant
- 2008-04-16 PT PT87459343T patent/PT2134685E/pt unknown
- 2008-04-16 CA CA2951295A patent/CA2951295C/fr active Active
-
2011
- 2011-04-15 US US13/088,206 patent/US8853209B2/en active Active
-
2014
- 2014-03-04 JP JP2014041214A patent/JP5895011B2/ja not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| EP2134685B1 (fr) | 2015-09-02 |
| CA2682354A1 (fr) | 2008-10-30 |
| ES2550753T3 (es) | 2015-11-12 |
| CN101711235A (zh) | 2010-05-19 |
| US20110263599A1 (en) | 2011-10-27 |
| DK2134685T3 (en) | 2015-12-07 |
| PT2134685E (pt) | 2015-11-25 |
| US7981888B2 (en) | 2011-07-19 |
| EP2134685A1 (fr) | 2009-12-23 |
| CA2951295A1 (fr) | 2008-10-30 |
| CA2951295C (fr) | 2020-04-28 |
| JP2010524955A (ja) | 2010-07-22 |
| MX2009011210A (es) | 2009-10-30 |
| US8853209B2 (en) | 2014-10-07 |
| US20090124616A1 (en) | 2009-05-14 |
| JP2014129396A (ja) | 2014-07-10 |
| JP5895011B2 (ja) | 2016-03-30 |
| JP5496876B2 (ja) | 2014-05-21 |
| CA2682354C (fr) | 2016-12-13 |
| WO2008130970A1 (fr) | 2008-10-30 |
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